Quality Operations Specialist

Job Summary: Seeking a Quality Operations Specialist to support pharmaceutical repackaging operations, quality inspections, labeling, documentation, and compliance with cGMP standards.

Requirements: ~ Bachelor’s degree in a science-related field. ~3+ years of pharmaceutical industry experience. ~ Experience in QA/QC within an FDA-regulated facility. ~ Medication repackaging experience preferred. ~ Knowledge of pharmaceutical labeling, inspections, deviations, and quality audits. ~ Experience with controlled substances, DEA Form 222, and ARCOS is a plus. ~ Strong attention to detail and documentation skills. ~ Proficiency with Microsoft Office and Share Point. ~ Reliable transportation and ability to work onsite starting at 6:00 AM. ~ Ability to lift up to 30 lbs. as needed.

Responsibilities: Perform incoming, in-process, and final quality inspections. Create and update pharmaceutical labels and drug information. Maintain quality and training documentation. Support deviations, investigations, and quality audits. Track controlled substances and maintain required records. Support drug destruction and retain sample audits. Report quality issues and out-of-specification results to management. Pre-Screen Questions What is your degree and field of study? How many years of pharmaceutical experience do you have? Describe your FDA-regulated QA/QC experience. Do you have medication repackaging experience? Do you have experience with DEA Form 222, ARCOS, deviations, or audits? Can you work onsite Monday–Friday, 6:00 AM–2:30 PM? Do you require sponsorship now or in the future? Are you comfortable with the stated pay and temp-to-hire structure? When can you start?

Employment Type: Full Time

Salary: $21 - $25 Hourly Bonus/Commission: No